Evidence map›Paper›PMID 42179116›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Generalized Analysis of Electrophilic Small Molecules.

Uma Neelakantan, Maowei Hu, Jiya Bhatia, Huyen N Nguyen, John Bobby Yeboah, Eirinaios I Vrettos, Dionysius Copoulos, Khue N M Nguyen, Madan M Babu, Daniel J Blair

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Uma NeelakantanDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Maowei HuDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Jiya BhatiaDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Huyen N NguyenDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
John Bobby YeboahDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Eirinaios I VrettosDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Dionysius CopoulosDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Khue N M NguyenDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Madan M BabuCenter of Excellence for Data Driven Discovery, Department of Structural Biology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Daniel J BlairDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.ORCID https://orcid.org/0000-0002-2279-7538

Funding

PROFESSIONAL ONCOLOGY EDUCATION PROGRAMR25CA023944 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SUZANNE A. GRONEMEYER · 1986 to 2026
$8.3M
Developing and Discovering Covalent Inhibitors through Fragmentation-First ExperimentationR35GM159997 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BLAIR, DANIEL JAMES · 2025 to 2025
$2.5M
American Lebanese Syrian Associated CharitiesNCI NIH HHS R25 CA023944NIGMS NIH HHS R35 GM159997NIH HHS R35GM159997Pediatric Oncology Education Program R25CA23944
6 · The paper itself

Abstract

Chemical construction almost universally employs highly customized product-specific analytics. A transition toward generality will remove this critical bottleneck. Here we present how the fundamental chemical property of electrophilicity can be leveraged to generalize reaction analytics. By using a simple thiol probe we transform customized analytical schemes for electrophilic small molecules into a single generalized readout by tandem mass spectrometry. We apply this strategy to acrylamides commonly found in covalent inhibitors, and subsequently show how it can be extended to other classes of electrophilic small molecules. Application of this approach to high-throughput chemical synthesis streamlines analysis, enabling rapid readouts of chemical analogs featuring acrylamides.

Indexed as

acoustic ejectioncovalent inhibitorelectrophilic warheadhigh‐throughput experimentationmass‐spectrometrytandem mass‐spectrometry

Identifiers

PMID42179116
PMCPMC13340528

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.